CTTM07 - Step-by-step guide (High-level admin)

Classified as internal/staff & contractors by the European Medicines Agency Step-by-step guide European Medicines Agency, 2021 Reproduction and/or distribution of the content of these training materials for non-commercial or commercial purposes is authorised, provided the European Medicines Agency is acknowledged as the source of the European Medicines Agency developed this training material to enhance public access to information on the Clinical Trial Information System (CTIS). This material describes a preliminary version of CTIS and may therefore not entirely describe the system as it is at the time of use of this material. The Agency does not warrant or accept any liability in relation to the use (in part or in whole) or the interpretation of the information contained in this training material by third of roles and permissionsHigh-level Administrator registrationCTIS Training Programme Module 07 Version October 2022 Learning Objectives Understandhowto as internal/staff & contractors by the European Medicines Agency Record of updated versions CTIS for SMEs and Academia The table below describes the updated versions after CTIS go-live (January 2022) the training material to

The Sponsor Administrators are the High-level Administrators in the sponsor workspace; while the Member State Administrators and the European Commission Administrators are the High-level Administrators in the authority workspace. This step-by-step guide explains the steps to request High-level Administrator roles via the IAM process. Request a

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